documents: FDA-2000-N-0108-0023
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | agency_id | docket_id | title | document_type | subtype | posted_date | posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-2000-N-0108-0023 | FDA | FDA-2000-N-0108 | Reference 12 - "Department of Health and Human Services, Office of the Inspector General, Review of the Food and Drug Administration’s Handling of Adverse Drug Reaction Reports, Report No. A-15-98-50001, 1999" - [Safety Reporting Requirements for Human Drug and Biological Products; NPR1] re FDA-2000-N-0108-0006 | Supporting & Related Material | Background Material | 2010-02-26T05:00:00Z | 2010 | 2 | 2016-02-25T16:35:47Z | 0 | 0 | 09000064804c26f1 |
Links from other tables
- 0 rows from regs_document_id in fr_regs_crossref